rs11568563
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs11568563(A;C) |
| Make rs11568563(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 12 |
| Position | 21304500 |
| Gene | SLCO1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11568563 |
| dbSNP (classic) | rs11568563 |
| ClinGen | rs11568563 |
| ebi | rs11568563 |
| HLI | rs11568563 |
| Exac | rs11568563 |
| Gnomad | rs11568563 |
| Varsome | rs11568563 |
| LitVar | rs11568563 |
| Map | rs11568563 |
| PheGenI | rs11568563 |
| Biobank | rs11568563 |
| 1000 genomes | rs11568563 |
| hgdp | rs11568563 |
| ensembl | rs11568563 |
| geneview | rs11568563 |
| scholar | rs11568563 |
| rs11568563 | |
| pharmgkb | rs11568563 |
| gwascentral | rs11568563 |
| openSNP | rs11568563 |
| 23andMe | rs11568563 |
| SNPshot | rs11568563 |
| SNPdbe | rs11568563 |
| MSV3d | rs11568563 |
| GWAS Ctlg | rs11568563 |
| GMAF | 0.03352 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21685912 ]
|
| Trait | |
| Title | Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. |
| Risk Allele | |
| P-val | 7E-8 |
| Odds Ratio | 1.4700 [1.28-1.69] |
